Allele Registry

Canonical Allele Identifier: PA124254

Gene: INSR HGNC NCBI

ClinVar RCV:

RCV000015817

ClinVar Variation:

14702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001073285.1:p.Val55Ala	CA124253 NM_001079817.3:c.164T>C